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University of Sheffield
ENERGY MIGRATION AND TRANSFER IN LIGHT EMITTING POLYMER SYSTEMS. Jonathan Hill University of Sheffield (UK)
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Overview Introduction - definition of terms and aim of experiment
Experimental technique. Results : 1. Migration in F8 2. Transfer in layered films 3. Transfer in blended films Conclusions Acknowledgements
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Introduction Förster Transfer :
Non-radiative (resonance) mechanism for transferring energy from one material (donor) to another (acceptor), mediated by the Coulomb force. Depends on distance between the molecules (1/R6) and the orientation of their transition dipoles. Energy migration : Excitations can “migrate” to lower energy sites via the Förster mechanism, observed as a red-shift in fluorescence with time.
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Introduction Light Emitting Polymer :
Organic material that consists of many repeat units, whose excitations decay radiatively. Two such polymers are : Poly(9,9-dioctylfluorene) (F8) Poly(9,9-dioctylfluorene-co-benzothiadiazole) (BT)
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Experimental Technique
Time-resolved photoluminescence (PL) measurements were taken to determine the rates of migration and transfer. Samples were excited using a 100fs pulsed Ti:sapphire laser.
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Results (1) Migration in F8 was investigated as a function of temperature : The PL spectra were modelled with gaussian curves. Distribution of excited states increases with temperature, i.e. increased migration.
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Results (1) Peak position shifts more at low temperatures – contradicts previous result? Low T - excitons migrate easily to lower energy so peak red-shifts as expected. High T - thermal scattering allows excitons to migrate to higher energy states. i.e. at high T, average exciton energy remains more static but distribution of energies is increased.
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Results (2) Energy transfer from F8 to BT was investigated as a function of donor-acceptor separation. Layered structures were prepared which allowed precise control over donor-acceptor separation. BT - spin cast onto silicon. Stearic acid (SAC) - deposited via Langmuir-Blodgett (LB) technique. (Optically inert layers of known thickness.) F8 - deposited via fast LB technique
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Results (2) The lifetime of the donor (F8) fluorescence was measured for a number of samples with varying spacer layer thicknesses. Samples with larger spacer layers exhibited a longer donor lifetime due to reduced energy transfer between polymers. The sample with no spacer layers exhibited a lifetime of ~60ps, c.f. pure donor lifetime of ~105ps. Two sample decays are shown above - note that decays are single exponential.
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Results (3) Blended spin cast samples were prepared by mixing the required concentration of F8 and BT in solution. Transfer as a function of guest concentration was investigated. Observed donor decay dynamics are different than those in the layered structures. Decays are no longer exponential in shape – attributed to increased migration affecting the Förster rate. Typical PL decays from blend samples. Solid lines are fitted single exponentials.
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Conclusions Energy migration occurs in F8 over a timescale of ~500ps.
The sample structure affects how energy transfer proceeds. Layered structures give exponential donor decays. Blended samples give non-exponential donor decays. This has implications for understanding the energy transfer process in many real-world applications, such as polymer LEDs.
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Acknowledgements Dr. Mark Fox Dr. Tim Richardson Prof. Donal Bradley
Miss Sasha Heriot
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